Ethyl 6-bromo-3-hydroxy-5-methylpyrazine-2-carboxylate

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Reagent Code: #184288
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CAS Number 1269026-22-3

science Other reagents with same CAS 1269026-22-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 261.07 g/mol
Formula C₈H₉BrN₂O₃
badge Registry Numbers
MDL Number MFCD29905280
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of antihypertensive and antiviral drugs. Its functional groups enable selective modifications, making it valuable in constructing complex heterocyclic systems. Commonly employed in medicinal chemistry for building pyrazine-based scaffolds that exhibit biological activity. Also utilized in research settings to design enzyme inhibitors and receptor modulators due to its structural compatibility with bioactive molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿720.00
inventory 1g
10-20 days ฿1,820.00
inventory 250mg
10-20 days ฿940.00
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Ethyl 6-bromo-3-hydroxy-5-methylpyrazine-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of antihypertensive and antiviral drugs. Its functional groups enable selective modifications, making it valuable in constructing complex heterocyclic systems. Commonly employed in medicinal chemistry for building pyrazine-based scaffolds that exhibit biological activity. Also utilized in research settings to design enzyme inhibitors and receptor modulators due to its structural compatibility with bioact

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of antihypertensive and antiviral drugs. Its functional groups enable selective modifications, making it valuable in constructing complex heterocyclic systems. Commonly employed in medicinal chemistry for building pyrazine-based scaffolds that exhibit biological activity. Also utilized in research settings to design enzyme inhibitors and receptor modulators due to its structural compatibility with bioactive molecules.

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